SYSTEMS AND METHODS FOR IDENTIFYING SOMATIC MUTATIONS

Methods and materials for assessing allelic imbalance

Method and apparatus for performing similarity searching

Genomic infrastructure for on-site or cloud-based DNA and RNA processing and analysis

FOOD PATHOGEN BIOINFORMATICS

Method for designing RNA binding protein utilizing PPR motif, and use thereof

DNA alignment using a hierarchical inverted index table

Methods and systems for storing sequence read data

Methods for determining lymphocyte receptor chain pairs

High throughput screening of populations carrying naturally occurring mutations

VARIANT ANALYSIS IN HIGH-THROUGHPUT SEQUENCING APPLICATIONS

Method For Using Protein Databases To Identify Microorganisms

Methods for the Determination of a Copy Number of a Genomic Sequence in a Biological Sample

PREFIX BURROWS-WHEELER TRANSFORMATIONS FOR CREATING AND SEARCHING A MERGED LEXEME SET

ANALYSIS OF A POLYMER FROM MULTI-DIMENSIONAL MEASUREMENTS

Biological state machines

MODEL ADJUSTMENT DURING ANALYSIS OF A POLYMER FROM NANOPORE MEASUREMENTS

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

SYSTEM AND METHOD FOR AUTOMATING DATA GENERATION AND DATA MANAGEMENT FOR A NEXT GENERATION SEQUENCER

Adaptive compression and modification of nanopore measurement data

Healthcare analysis stream management

Methods for non-invasive prenatal ploidy calling

METHOD FOR INCREASING UTILIZATION OF GENETIC TESTING

Algorithm for constructing hypothetical evolutionary trees using common mutations similarity matrices

METHOD FOR DETECTING CARCINOGENESIS IN THE UTERINE CERVIX

Detecting mutations for cancer screening

Machine learning for somatic single nucleotide variant detection in cell-free tumor nucleic acid sequencing applications

Bambam: parallel comparative analysis of high-throughput sequencing data

METHOD AND PROCESS FOR WHOLE GENOME SEQUENCING FOR GENETIC DISEASE DIAGNOSIS

METHODS AND KITS FOR SEQUENCING AND CHARACTERIZING PROTOZOA

Systems and methods for epigenetic analysis

Methods and systems for identifying CRISPR/Cas off-target sites

Method and system for multiplex primer design

Identification of surface-associated antigens for tumor diagnosis and therapy

HIGHLY MULTIPLEX PCR METHODS AND COMPOSITIONS

Method and composition for diagnosis or treatment of aggressive prostate cancer

DNA sequencing using MOSFET transistors

Method and device for mutation prioritization for personalized therapy

High throughput genome-wide translocation sequencing

Single-molecule sequencing of plasma DNA

Capture primers and capture sequence linked solid supports for molecular diagnostic tests

Method for identifying novel minor histocompatibility antigens

Resolving genome fractions using polymorphism counts

Compositions, processes and algorithms for microbial detection

Methods for determining fraction of fetal nucleic acids in maternal samples

Systems, compositions, and methods for discovery of MSI and neoepitopes that predict sensitivity to checkpoint inhibitors

Method and arrangement for matching mammals by comparing genotypes

Stable proteins and methods for designing same

Methylation pattern analysis of haplotypes in tissues in a DNA mixture

System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals

DISTANCE MAPS USING MULTIPLE ALIGNMENT CONSENSUS CONSTRUCTION

Analysis of fragmentation patterns of cell-free DNA

High throughput screening of populations carrying naturally occurring mutations

ANCESTRAL-SPECIFIC REFERENCE GENOMES AND METHODS OF CONSTRUCTING

ANCESTRAL-SPECIFIC REFERENCE GENOMES AND USES IN SELECTING AN EGG, EMBRYO, OR SPERM

ANCESTRAL-SPECIFIC REFERENCE GENOMES AND USES IN IDENTIFYING AN INDIVIDUAL ATTRIBUTE

ANCESTRAL-SPECIFIC REFERENCE GENOMES AND USES IN DETERMINING RESPONSE TO AN ACTIVE AGENT

Ancestral-specific reference genomes and uses in determining prognosis

Local genetic ethnicity determination system

Ancestral-specific reference genomes and uses in identifying a candidate for a clinical trial

Sequence data analyzer, DNA analysis system and sequence data analysis method

ANCESTRAL-SPECIFIC REFERENCE GENOMES AND USES IN SEQUENCING

MDM2-containing double minute chromosomes and methods therefore

METHODS FOR NON-INVASIVE PRENATAL PLOIDY CALLING

Device, system and method for securing and comparing genomic data

METHODS AND APPARATUSES FOR GENERATING REFERENCE GENOME DATA, GENERATING DIFFERENCE GENOME DATA, AND RECOVERING DATA

Multi-targeting short interfering RNAs

Genetic markers associated with suicide risk and methods of use thereof

Master Transcription Factors Identification and Use Thereof

PROCESSING AND ANALYSIS OF COMPLEX NUCLEIC ACID SEQUENCE DATA

Systems and Methods for Multi-Scale, Annotation-Independent Detection of Functionally-Diverse Units of Recurrent Genomic Alteration

Scar-less multi-part DNA assembly design automation

Sequencing using concatemers of copies of sense and antisense strands

Digital counting of individual molecules by stochastic attachment of diverse labels

METHODS FOR ALLELE CALLING AND PLOIDY CALLING

METHODS OF PREDICTING PATHOGENICITY OF GENETIC SEQUENCE VARIANTS

Computer systems and methods for genomic analysis

METHODS FOR NON-INVASIVE PRENATAL PLOIDY CALLING

System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals

METHODS FOR INTRODUCING MUTATIONS THAT ALTER THE PROBABILITY OF INTRANUCLEIC ACID BASE PAIRING OF A CONSERVED STRUCTURED NUCLEOTIDE AND RELATED COMPOSITIONS

SYSTEMS AND METHODS FOR IDENTIFYING MICROORGANISMS

Systems and methods for classifying, prioritizing and interpreting genetic variants and therapies using a deep neural network

Methods and systems for genetic analysis

Method for the deconvolution of nucleic acid-containing substance mixtures

Amplification assay with a probe competitor

Methods of storing information using nucleic acids

Methods for non-invasive prenatal ploidy calling

A FRAMEWORK FOR DETERMINING THE RELATIVE EFFECT OF GENETIC VARIANTS

Discovering population structure from patterns of identity-by-descent

De novo diploid genome assembly and haplotype sequence reconstruction

DISEASE-ASSOCIATED GENETIC VARIATIONS AND METHODS FOR OBTAINING AND USING SAME

Optimized Fc variants and methods for their generation

Compression and transmission of genomic information

Methods for the graphical representation of genomic sequence data

Method and system for microbiome-derived diagnostics and therapeutics for endocrine system conditions

Methods for the analysis of high resolution melt curve data

Methods and systems for copy number variant detection

Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing

METHODS FOR EVALUATING NEUROLOGICAL DISEASE

Methods And Systems For Detecting Genetic Mutations

Systems and methods for genomic variant annotation

System and method for construction of internal controls for improved accuracy and sensitivity of DNA testing

Detecting cancer mutations and aneuploidy in chromosomal segments

METHODS OF WEIGHT ANALYSIS AND USES THEREOF

MOLECULAR SIGNATURES OF CONDITIONS ASSOCIATED WITH LONGEVITY

Measurement and comparison of immune diversity by high-throughput sequencing

Barcode sequences, and related systems and methods

Computational Methods for Translating a Sequence of Multi-Base Color Calls to a Sequence of Bases

Method to match organ donors to recipients for transplantation

Transcript Determination Method

Compositions and methods for diagnosing, evaluating and treating cancer

Method of determining disease causality of genome mutations

Digital counting of individual molecules by stochastic attachment of diverse labels

Methods and systems for obtaining a single molecule consensus sequence

GENETIC VARIANTS AS MARKERS FOR USE IN DIAGNOSIS, PROGNOSIS AND TREATMENT OF EOSINOPHILIA, ASTHMA AND MYOCARDIAL INFARCTION

Error suppression in sequenced DNA fragments using redundant reads with unique molecular indices (UMIS)

Biomolecule sequencing devices, systems and methods

Antibody identification by lineage analysis

Optimized Fc variants and methods for their generation

SAMPLE INDEXING METHODS AND COMPOSITIONS FOR SEQUENCING APPLICATIONS

Methods and systems for variant detection

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

Methods and systems for detecting sequence variants

Healthcare analysis stream management

Genome compression and decompression

MOLECULAR PROFILING OF TUMORS

Methods, systems and processes of identifying genetic variation in highly similar genes

METHOD FOR SIMULTANEOUS DETECTION OF GENOME-WIDE COPY NUMBER CHANGES, cnLOH, INDELS, AND GENE MUTATIONS

System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals

Polymorphic gene typing and somatic change detection using sequencing data

Methods for full-length amplification of double-stranded linear nucleic acids of unknown sequences

Haplotype Based Generalizable Allele Specific Silencing for Therapy of Cardiovascular Disease

Non-invasive assessment of chromosome alterations using change in subsequence mappability

Synthetic biology tools

A METHOD OF GENERATING A REFERENCE INDEX DATA STRUCTURE AND METHOD FOR FINDING A POSITION OF A DATA PATTERN IN A REFERENCE DATA STRUCTURE

HCV GENOTYPING ALGORITHM

T cell receptor and B cell receptor repertoire analysis system, and use of same in treatment and diagnosis

Method for evaluating minority variants in a sample

Computation pipeline of location-dependent variant calls

Computation pipeline of single-pass multiple variant calls

Method and system for genomic visualization

METHODS AND SYSTEMS FOR SCREENING DISEASES IN SUBJECTS

BamBam: parallel comparative analysis of high-throughput sequencing data

Bambam: parallel comparative analysis of high-throughput sequencing data

Methods for genome assembly and haplotype phasing

Bambam: parallel comparative analysis of high-throughput sequencing data

METHODS AND COMPOSITIONS FOR POOLING AMPLIFICATION PRIMERS

SYSTEMS AND METHODS FOR ANALYZING NUCLEIC ACID

Diagnostic miRNA markers for Alzheimer

Integrated devices and systems for free-space optical coupling

Telemetrics and alert system

Performing sequence analysis as a relational join

Methods for Detection of Fetal Chromosomal Abnormality Using High Throughput Sequencing

METHOD AND SYSTEM OF MAPPING SEQUENCING READS

METHOD AND DEVICE FOR OPTIMIZING A NUCELOTIDE SEQUENCE FOR THE PURPOSE OF EXPRESSION IN A PROTEIN

Systems and methods for genomic pattern analysis

SYSTEMS AND METHODS FOR GENETIC TESTING ALGORITHMS

Sequential sequencing

Sequential sequencing

Systems and methods to detect rare mutations and copy number variation

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

Nucleic acid sequence assembly

MULTI-SAMPLE DIFFERENTIAL VARIATION DETECTION

NUCLEIC ACID COPY NUMBER DETERMINATION BASED ON FRAGMENT ESTIMATES

COMPUTER IMPLEMENTED METHOD FOR INDEXING REFERENCE GENOME

Method for large scale scaffolding of genome assemblies

Methods for obtaining a single molecule consensus sequence

Method and system for microbiome-derived diagnostics and therapeutics for endocrine system conditions

Systems and methods for determining structural variation and phasing using variant call data

Analyzing copy number variation in the detection of cancer

High-order sequence kernel methods for peptide analysis

Method and system for microbiome-derived diagnostics and therapeutics for conditions associated with microbiome functional features

DEVICES AND METHODS FOR DIAGNOSTICS BASED ON ANALYSIS OF NUCLEIC ACIDS

Methods of Selection, Reporting and Analysis of Genetic Markers Using Broad-Based Genetic Profiling Applications

Methods and Workflows for Selecting Genetic Markers Utilizing Software Tool

Digital counting of individual molecules by stochastic attachment of diverse labels

Combined size- and count-based analysis of maternal plasma for detection of fetal subchromosomal aberrations

IDENTIFYING MOLECULAR SYSTEMS IN PROTEIN SEQUENCE DATA

Proteomics analysis and discovery through DNA and RNA sequencing, systems and methods

Spray nozzle for fluidized catalytic cracking

Detecting and classifying copy number variation

METHODS OF QUALITY CONTROL USING SINGLE-NUCLEOTIDE POLYMORPHISMS IN PRE-IMPLANTATION GENETIC SCREENING

Method and system for determining cancer status

SYSTEMS AND METHODS FOR IDENTIFYING STRUCTURALLY OR FUNCTIONALLY SIGNIFICANT NUCLEOTIDE SEQUENCES

Method of nuclear DNA and mitochondrial DNA analysis

Digital measurements from targeted sequencing

DNA sequencing using MOSFET transistors

SYSTEMS AND METHODS FOR IDENTIFYING STRUCTURALLY OR FUNCTIONALLY SIGNIFICANT AMINO ACID SEQUENCES

Genome browser

ANALYSIS OF POLYNUCLEOTIDES

Noninvasive prenatal diagnosis of fetal trisomy by allelic ratio analysis using targeted massively parallel sequencing

Single molecule-overlapping read analysis for minor variant mutation detection in pathogen samples

Variety identification-encoding system and encoding method using the same

Detecting and classifying copy number variation

Method and system for high-throughput sequencing data analysis

METHODS OF CHARACTERIZING, DETERMINING SIMILARITY, PREDICTING CORRELATION BETWEEN AND REPRESENTING SEQUENCES AND SYSTEMS AND INDICATORS THEREFOR

Systems and Methods for Error Correction in DNA Sequencing

Methods and Compositions for the Detection, Classification, and Diagnosis of Schizophrenia

Transcriptome-wide design of selective, bioactive small molecules targeting RNA

Non-invasive prenatal diagnosis of fetal genetic condition using cellular DNA and cell free DNA

METHOD AND SYSTEM FOR EVALUATING SEQUENCES

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

MOLECULAR AND BIOINFORMATICS METHODS FOR DIRECT SEQUENCING

MOLECULAR PROFILING OF TUMORS

ENHANCED DETECTION OF NON-SOMATIC CIRCULATING NUCLEIC ACIDS

Bioinformatics Systems, Apparatuses, And Methods Executed On An Integrated Circuit Processing Platform

Methods for non-invasive prenatal ploidy calling

METHOD FOR DETERMINING READ ERROR IN NUCLEOTIDE SEQUENCE

Windowed sequencing

TREATMENT OF INSULIN GENE (INS) RELATED DISEASES BY INHIBITION OF NATURAL ANTISENSE TRANSCRIPT TO AN INSULIN GENE (INS)

System and method for inter-species DNA mixture interpretation

METHOD AND SYSTEM FOR DETERMINING A BACTERIAL RESISTANCE TO AN ANTIBIOTIC DRUG

ANALYSIS OF A POLYMER COMPRISING POLYMER UNITS

METHODS FOR MODELING CHINESE HAMSTER OVARY (CHO) CELL METABOLISM

METHOD AND DEVICE FOR DETECTING CHROMOSOMAL ANEUPLOIDY

METHODS FOR IDENTIFICATION OF INDIVIDUALS

NEXT GENERATION SEQUENCING ANALYSIS SYSTEM AND NEXT GENERATION SEQUENCING ANALYSIS METHOD THEREOF

SYSTEMS, METHODS, AND ENVIRONMENT FOR AUTOMATED REVIEW OF GENOMIC DATA TO IDENTIFY DOWNREGULATED AND/OR UPREGULATED GENE EXPRESSION INDICATIVE OF A DISEASE OR CONDITION

Methods and systems for storing sequence read data

Rice whole genome breeding chip and application thereof

APPARATUS AND METHOD FOR COUNTING ALLELES

RATIONAL METHOD FOR SOLUBILISING PROTEINS

Microbial markers and uses therefor

Strategies for high throughput identification and detection of polymorphisms

Methods and materials for assessing allelic imbalance

Systems and Methods for Sequence Data Alignment Quality Assessment

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

VARIANT CALLER

METHOD FOR FORMING PERSONAL NUTRITION COMPLEX ACCORDING TO INCIDENCE OF DISEASE AND GENETIC POLYMORPHISM BY A PREDICTION SYSTEM

SYSTEM AND METHODS FOR DETERMINING A WOMAN'S RISK OF ANEUPLOID CONCEPTION

Sequence-centric scientific information management

Construction of diverse synthetic peptide and polypeptide libraries

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

NOISE MODEL TO DETECT COPY NUMBER ALTERATIONS

Managing gene sequences

Method for privacy-preserving medical risk test

POOL TEST RESULT VERIFICATION METHOD AND APPARATUS

METHOD FOR ASSIGNING TARGET-ENRICHED SEQUENCE READS TO A GENOMIC LOCATION

Accurate typing of HLA through exome sequencing

Genetic test

METHOD FOR QUANTIFYING THE LEVEL OF MINIMAL RESIDUAL DISEASE IN A SUBJECT

METHODS FOR DETERMINING ABSOLUTE GENOME-WIDE COPY NUMBER VARIATIONS OF COMPLEX TUMORS

Bioinformatics process for identifying at risk subject populations

Determination of TGF-β pathway activity using unique combination of target genes

Secure and scalable mapping of human sequencing reads on hybrid clouds

METHODS, SYSTEMS, AND COMPUTER-READABLE MEDIA FOR BLIND DECONVOLUTION DEPHASING OF NUCLEIC ACID SEQUENCING DATA

METHODS AND SYSTEMS FOR ALIGNING REPETITIVE DNA ELEMENTS

Methods and processes for non-invasive assessment of genetic variations

Performing sequence analysis as a relational join

Methods for calculating corrected amplicon coverages

BIOLOGICAL SEQUENCE VARIANT CHARACTERIZATION

BIOLOGICAL SEQUENCE TANDEM REPEAT CHARACTERIZATION

Biological sequence variant characterization

BIOLOGICAL SEQUENCE TANDEM REPEAT CHARACTERIZATION

Methods and Systems for Social Networking Based on Nucleic Acid Sequences

Apparatuses, methods, systems, and computer-readable media for fluid potential artifact correction in reagent delivery systems

Methods for sequencing polynucleotides

HLA typing using selective amplification and sequencing

APPARATUS AND METHOD FOR DETECTING INTERNAL TANDEM DUPLICATION

METHODS AND SYSTEMS FOR DETECTION OF A GENETIC MUTATION

Methods for sequence-directed molecular breeding

Methods and processes for calling bases in sequence by incorporation methods

METHODS AND SYSTEMS FOR GENOME ANALYSIS

Accurate and fast mapping of reads to genome

Method and device for detecting chromosomal structural abnormalities

METHODS AND SYSTEMS FOR ANALYZING NUCLEIC ACID SEQUENCING DATA

System, method and computer-accessible medium for secure and compressed transmission of genomic data

Method and apparatus for DNA-based authentication system

Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform

METHOD OF AND APPARATUS FOR PROVIDING INFORMATION ON A GENOMIC SEQUENCE BASED PERSONAL MARKER

FUSION TRANSCRIPT DETECTION METHODS AND FUSION TRANSCRIPTS IDENTIFIED THEREBY

Methods and systems for nucleic acid sequencing validation, calibration and normalization

VISUALIZING GENOMIC DATA

VARIANT-CALLING ON DATA FROM AMPLICON-BASED SEQUENCING METHODS

Systems And Methods For Determination Of Provenance

Aligning and clustering sequence patterns to reveal classificatory functionality of sequences

Detecting and classifying copy number variation

Method and apparatus for identification of biomolecules

Strategies for high throughput identification and detection of polymorphisms

METHOD AND APPARATUS FOR DETERMINING TRANSCRIPTION FACTOR FOR BIOLOGICAL PROCESS

METHODS FOR QUANTITATIVE GENETIC ANALYSIS OF CELL FREE DNA

Genetic information storage apparatus, genetic information search apparatus, genetic information storage program, genetic information search program, genetic information storage method, genetic information search method, and genetic information search system

Characterization of molecules in nanofluidics

Methods and nucleotide fragments of predicting occurrence, metastasis of cancers and patients' postoperative survival in vitro

SYSTEMS AND METHODS TO DETECT RARE MUTATIONS AND COPY NUMBER VARIATION

Systems And Methods For Baseline Correction Using Non-Linear Normalization

METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS

System and Method for Detecting Population Variation from Nucleic Acid Sequencing Data

METHOD FOR EVALUATING AN IMMUNOREPERTOIRE

OLIGONUCLEOTIDE PROBES FOR SPECIFIC IDENTIFICATION OF NOROVIRUSES AND OTHER PATHOGENS

Identification and Use of Circulating Nucleic Acid Tumor Markers

METHOD OF ESTABLISHING A GENETIC RISK STRATIFICASTION FOR GENETIC ADDICTION RISK ANALYSIS

MicroRNAs and uses thereof

Systems and methods for identifying an individual

Detecting Chromosomal Aneuploidy

Methods and uses for molecular tags

Method and apparatus for calling single-nucleotide variations and other variations

METHOD AND APPARATUS FOR SEPARATING QUALITY LEVELS IN SEQUENCE DATA AND SEQUENCING LONGER READS